EconPapers    
Economics at your fingertips  
 

Benchmarking the negatives: Effect of negative data generation on the classification of miRNA-mRNA interactions

Efrat Cohen-Davidi and Isana Veksler-Lublinsky

PLOS Computational Biology, 2024, vol. 20, issue 8, 1-25

Abstract: MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression post-transcriptionally. In animals, this regulation is achieved via base-pairing with partially complementary sequences on mainly 3’ UTR region of messenger RNAs (mRNAs). Computational approaches that predict miRNA target interactions (MTIs) facilitate the process of narrowing down potential targets for experimental validation. The availability of new datasets of high-throughput, direct MTIs has led to the development of machine learning (ML) based methods for MTI prediction. To train an ML algorithm, it is beneficial to provide entries from all class labels (i.e., positive and negative). Currently, no high-throughput assays exist for capturing negative examples. Therefore, current ML approaches must rely on either artificially generated or inferred negative examples deduced from experimentally identified positive miRNA-target datasets. Moreover, the lack of uniform standards for generating such data leads to biased results and hampers comparisons between studies. In this comprehensive study, we collected methods for generating negative data for animal miRNA–target interactions and investigated their impact on the classification of true human MTIs. Our study relies on training ML models on a fixed positive dataset in combination with different negative datasets and evaluating their intra- and cross-dataset performance. As a result, we were able to examine each method independently and evaluate ML models’ sensitivity to the methodologies utilized in negative data generation. To achieve a deep understanding of the performance results, we analyzed unique features that distinguish between datasets. In addition, we examined whether one-class classification models that utilize solely positive interactions for training are suitable for the task of MTI classification. We demonstrate the importance of negative data in MTI classification, analyze specific methodological characteristics that differentiate negative datasets, and highlight the challenge of ML models generalizing interaction rules from training to testing sets derived from different approaches. This study provides valuable insights into the computational prediction of MTIs that can be further used to establish standards in the field.Author summary: Gene expression regulation is fundamental for all organisms’ development, homeostasis, and environmental adaptation. microRNAs (miRNAs) play a central role in post-transcriptional gene regulation by binding to target mRNAs and repressing their translation or mediating their degradation. Technical challenges in experimental miRNA target identification led to growing interest in computational target prediction. While machine learning (ML) models have shown success in this area, they rely heavily on artificially generated negative examples due to limited experimental data. The diversity of methods for generating negative interactions and the lack of a uniform standardized approach introduce bias and hinder the comparison of results across different studies.

Date: 2024
References: View complete reference list from CitEc
Citations:

Downloads: (external link)
https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1012385 (text/html)
https://journals.plos.org/ploscompbiol/article/fil ... 12385&type=printable (application/pdf)

Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.

Export reference: BibTeX RIS (EndNote, ProCite, RefMan) HTML/Text

Persistent link: https://EconPapers.repec.org/RePEc:plo:pcbi00:1012385

DOI: 10.1371/journal.pcbi.1012385

Access Statistics for this article

More articles in PLOS Computational Biology from Public Library of Science
Bibliographic data for series maintained by ploscompbiol ().

 
Page updated 2025-05-04
Handle: RePEc:plo:pcbi00:1012385